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Clinical trial of YAG laser vitreolysis for floater caused by Weiss ring

Clinical trial of YAG laser vitreolysis for Weiss ring after posterior vitreous detachment - Clinical trial of YAG laser vitreolysis for Weiss ring after posterior vitreous detachment

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000036588
Enrollment
75
Registered
2019-04-24
Start date
2017-03-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

floater caused by Weiss ring

Interventions

YAG laservitreolysis sham YAG laser

Sponsors

The Study Group for Laser Vitreolysis
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) at least 6 month of symptom associated with floaters 2) posterior vitreous detachment confirmed by clinical examination, OCT and ultrasound B scan 3) more than 4 on the score of visual disturbance due to floaters (0 = no symptom, 10 = intolerable) 4) Weiss ring more than 3 mm away from the retina and 5 mm away from the lens not applicable if pseudophakic patients) by B scan 5) able to take position for YAG laser 6) understands the risk of YAG laser resulting in retinal detachment, intraocular hemorrhage, retinal injury, cataract formation, optic disc injury, inflammation, and other events causing visual disturbance 7) willing to cooperate to the study protocol 8) only one eye for the study even if the patient had symptom in both eye 9) willing to sign informed consent

Exclusion criteria

Exclusion criteria: 1) fellow eye with best corrected visual acuity bellow 0.4(20/50) 2) history of retinal break, retinal detachment, uveitis in the study eye 3) history of diabetic retinopathy, macular edema, retinal vein occlusion, or aphakia in the study eye 4) ongoing treatment of glaucoma or ocular hypertension by more than 2 kinds of glaucoma topical medication, history of glaucoma surgery in the study eye

Design outcomes

Primary

MeasureTime frame
Subjective change measured by visual questionnaire

Secondary

MeasureTime frame
a) visual acuity b) ultrasound B scan c) optical coherence tomography; OCT d) fundus photo image e) slit lamp examination, indirect ophthalmoscope,intra ocular pressure f) National Eye Institute Visual Functioning Questionnaire 25(VFQ-25)

Countries

Japan

Contacts

Public ContactKeiko Misawa

The Study Group for Laser Vitreolysis Secretariat

study1@laser-vitreolysis.net090-6009-7912

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026